dbVar for Gene (Select 1811) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7097853	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 104,456,677-108,155,935 , GRCh38.p12 chr7: 104,816,230-108,515,491	RNU6-1322P, COG5, 57 more genes
nsv7097603	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,412,489-107,559,714 , GRCh38.p12 chr7: 107,772,044-107,919,269	LOC105375444, DLD, 3 more genes
nsv7097099	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 102,937,907-107,643,330 , GRCh38.p12 chr7: 103,297,460-108,002,885	SRPK2, SYPL1, 60 more genes
nsv6835181	copy number variation	1	nstd229	human		GRCh38 chr7: 107,796,700-107,796,792 , GRCh37.p13 chr7: 107,437,145-107,437,237	SLC26A3
nsv6831951	copy number variation	1	nstd229	human		GRCh38 chr7: 107,606,801-107,918,600 , GRCh37.p13 chr7: 107,247,246-107,559,045	WBP1LP2, SLC26A4-AS1, 11 more genes
nsv6830887	copy number variation	1	nstd229	human		GRCh38 chr7: 107,795,460-107,797,900 , GRCh37.p13 chr7: 107,435,905-107,438,345	SLC26A3
nsv6828603	copy number variation	1	nstd229	human		GRCh38 chr7: 107,770,269-108,588,414 , GRCh37.p13 chr7: 107,410,714-108,228,858	LOC105375444, DLD, 15 more genes
nsv6825210	copy number variation	1	nstd229	human		GRCh38 chr7: 107,733,601-107,770,200 , GRCh37.p13 chr7: 107,374,046-107,410,645	CBLL1-AS1, CBLL1, 1 more genes
nsv6634332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635	RRBP1P1, SLC29A4P1, 2680 more genes
nsv6619821	copy number variation	1	nstd223	human		GRCh38 chr7: 107,759,301-107,763,800 , GRCh37.p13 chr7: 107,399,746-107,404,245	CBLL1, SLC26A3
nsv6606396	copy number variation	1	nstd223	human		GRCh38 chr7: 107,794,034-107,807,824 , GRCh37.p13 chr7: 107,434,479-107,448,269	SLC26A3, PIGCP2
nsv6573625	inversion	1	nstd223	human		GRCh38 chr7: 107,788,295-107,788,683 , GRCh37.p13 chr7: 107,428,740-107,429,128	SLC26A3
nsv6567430	inversion	1	nstd223	human		GRCh38 chr7: 107,773,839-107,774,280 , GRCh37.p13 chr7: 107,414,284-107,414,725	SLC26A3
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	AOC1, ACHE, 2682 more genes
nsv6315107	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,425,758-107,429,261 , GRCh38 chr7: 107,785,313-107,788,816	SLC26A3
nsv6313851	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648	DOCK4-AS1, RPL3P8, 262 more genes
nsv6313576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106	LHFPL3-AS2, CTB-30L5.1, 233 more genes
nsv6313503	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253	GJC3, LAMB4, 237 more genes
nsv6302133	copy number variation	1	nstd186	human		GRCh37 chr7: 107,410,612-107,410,776 , GRCh38.p12 chr7: 107,770,167-107,770,331	SLC26A3
nsv6292446	mobile element insertion	1	nstd186	human		GRCh37 chr7: 107,412,419-107,412,470 , GRCh38.p12 chr7: 107,771,974-107,772,025	SLC26A3

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Number of Variants: 20

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